Pwp1 Variant Search Result - Rat Genome Database

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27 records found for search term Pwp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598251239	CV3901956	single nucleotide variant	NM_007062.3(PWP1):c.8G>C (p.Arg3Pro)	not specified [RCV005259196]	uncertain significance	12	107685907	107685907	Human		name
405658665	CV3311748	single nucleotide variant	NM_007062.3(PWP1):c.253A>G (p.Arg85Gly)	not specified [RCV004438260]	uncertain significance	12	107688736	107688736	Human		name
407473509	CV3464800	single nucleotide variant	NM_007062.3(PWP1):c.199C>T (p.Arg67Cys)	not specified [RCV004662766]	uncertain significance	12	107688682	107688682	Human		name
407473517	CV3464802	single nucleotide variant	NM_007062.3(PWP1):c.272A>G (p.Glu91Gly)	not specified [RCV004662768]	uncertain significance	12	107688755	107688755	Human		name
598251244	CV3901957	single nucleotide variant	NM_007062.3(PWP1):c.229G>C (p.Glu77Gln)	not specified [RCV005259197]	uncertain significance	12	107688712	107688712	Human		name
598251254	CV3901959	single nucleotide variant	NM_007062.3(PWP1):c.121G>A (p.Glu41Lys)	not specified [RCV005259199]	uncertain significance	12	107688496	107688496	Human		name
156106553	CV2217873	single nucleotide variant	NM_007062.3(PWP1):c.476A>G (p.Gln159Arg)	not specified [RCV004084042]	uncertain significance	12	107693070	107693070	Human		name
156114791	CV2268646	single nucleotide variant	NM_007062.3(PWP1):c.741G>C (p.Lys247Asn)	not specified [RCV004124051]	uncertain significance	12	107697594	107697594	Human		name
156028746	CV2278557	single nucleotide variant	NM_007062.3(PWP1):c.571G>A (p.Val191Met)	not specified [RCV004132989]	uncertain significance	12	107696542	107696542	Human		name
155962831	CV2308200	single nucleotide variant	NM_007062.3(PWP1):c.379G>T (p.Asp127Tyr)	not specified [RCV004164703]	uncertain significance	12	107692873	107692873	Human		name
329379136	CV2460180	single nucleotide variant	NM_007062.3(PWP1):c.835A>G (p.Asn279Asp)	not specified [RCV004273278]	uncertain significance	12	107702963	107702963	Human		name
401741221	CV2713418	single nucleotide variant	NM_007062.3(PWP1):c.824C>T (p.Ala275Val)	not specified [RCV004319036]	uncertain significance	12	107702952	107702952	Human		name
407473513	CV3464801	single nucleotide variant	NM_007062.3(PWP1):c.978G>T (p.Leu326Phe)	not specified [RCV004662767]	uncertain significance	12	107704648	107704648	Human		name
597763709	CV3592333	single nucleotide variant	NM_007062.3(PWP1):c.364G>C (p.Gly122Arg)	not specified [RCV004849603]	uncertain significance	12	107692858	107692858	Human		name
597763715	CV3592334	single nucleotide variant	NM_007062.3(PWP1):c.356C>T (p.Thr119Met)	not specified [RCV004849604]	uncertain significance	12	107692850	107692850	Human		name
597763719	CV3592335	single nucleotide variant	NM_007062.3(PWP1):c.899A>G (p.Asp300Gly)	not specified [RCV004849605]	uncertain significance	12	107703027	107703027	Human		name
597763723	CV3592336	single nucleotide variant	NM_007062.3(PWP1):c.641C>T (p.Thr214Ile)	not specified [RCV004849606]	uncertain significance	12	107697494	107697494	Human		name
598251249	CV3901958	single nucleotide variant	NM_007062.3(PWP1):c.578G>T (p.Trp193Leu)	not specified [RCV005259198]	uncertain significance	12	107696549	107696549	Human		name
156233309	CV2245247	single nucleotide variant	NM_007062.3(PWP1):c.1177C>G (p.Leu393Val)	not specified [RCV004107016]	uncertain significance	12	107709119	107709119	Human		name
156075222	CV2273270	single nucleotide variant	NM_007062.3(PWP1):c.1079C>T (p.Ala360Val)	not specified [RCV004132063]	uncertain significance	12	107708927	107708927	Human		name
156177750	CV2298241	single nucleotide variant	NM_007062.3(PWP1):c.1006C>T (p.His336Tyr)	not specified [RCV004160162]	uncertain significance	12	107704676	107704676	Human		name
156000806	CV2383275	single nucleotide variant	NM_007062.3(PWP1):c.1492C>T (p.Pro498Ser)	not provided [RCV004695742]\|not specified [RCV004222325]	uncertain significance	12	107712206	107712206	Human		name
405658647	CV3311742	single nucleotide variant	NM_007062.3(PWP1):c.1019G>A (p.Arg340Gln)	not specified [RCV004438254]	uncertain significance	12	107704689	107704689	Human		name
405658650	CV3311743	single nucleotide variant	NM_007062.3(PWP1):c.1060T>C (p.Ser354Pro)	not specified [RCV004438255]	uncertain significance	12	107704730	107704730	Human		name
405658653	CV3311744	single nucleotide variant	NM_007062.3(PWP1):c.1319C>T (p.Pro440Leu)	not specified [RCV004438256]	uncertain significance	12	107710433	107710433	Human		name
405658656	CV3311745	single nucleotide variant	NM_007062.3(PWP1):c.1391C>T (p.Ser464Phe)	not specified [RCV004438257]	uncertain significance	12	107710505	107710505	Human		name
405658662	CV3311747	single nucleotide variant	NM_007062.3(PWP1):c.1487A>G (p.Asp496Gly)	not specified [RCV004438259]	uncertain significance	12	107712201	107712201	Human		name

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